rs587781506

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6	BRCA2 variant considered pathogenic for breast cancer
(G;G)	0	common in clinvar

Make rs587781506(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32362594

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587781506
dbSNP (classic)	rs587781506
ClinGen	rs587781506
ebi	rs587781506
HLI	rs587781506
Exac	rs587781506
Gnomad	rs587781506
Varsome	rs587781506
LitVar	rs587781506
Map	rs587781506
PheGenI	rs587781506
Biobank	rs587781506
1000 genomes	rs587781506
hgdp	rs587781506
ensembl	rs587781506
geneview	rs587781506
scholar	rs587781506
google	rs587781506
pharmgkb	rs587781506
gwascentral	rs587781506
openSNP	rs587781506
23andMe	rs587781506
SNPshot	rs587781506
SNPdbe	rs587781506
MSV3d	rs587781506
GWAS Ctlg	rs587781506

Max Magnitude

6

ClinVar
Risk	rs587781506(A;A)
Alt	rs587781506(A;A)
Reference	Rs587781506(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32936731G>A
CLNSRC
CLNACC	RCV000129483.2, RCV000195555.3, RCV000240971.2,